Many authors have concluded that the Chiari malformation Type I (CM-I) is due to a smaller than normal posterior cranial fossa. In order to establish this smaller geometry as the cause of hindbrain herniation in a family, the authors of this paper performed volumetric analysis in a family found to have this malformation documented in 4 generations.
Members from this family found to have a CM-I by imaging underwent volumetric analysis of their posterior cranial fossa using the Cavalieri method.
No member of this family found to have CM-I on preoperative imaging had a posterior fossa that was significantly smaller than that of age-matched controls.
The results of this study demonstrate that not all patients with a CM-I will have a reduced posterior cranial fossa volume. Although the mechanism for the development of hindbrain herniation in this cohort is unknown, this manifestation can be seen in multiple generations of a familial aggregation with normal posterior fossa capacity.
Atkinson JL, , Kokmen E, & Miller GM: Evidence of posterior fossa hypoplasia in the familial variant of adult Chiari I malformation: case report. Neurosurgery 42:401–404, 1998
Badie B, , Mendoza D, & Batzdorf U: Posterior fossa volume and response to suboccipital decompression in patients with Chiari I malformation. Neurosurgery 37:214–218, 1995
Boyles AL, , Enterline DS, , Hammock PH, , Siegel DG, , Slifer SH, & Mehltretter L, et al.: Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15. Am J Med Genet A 15:2776–2785, 2006
Cavender RK, & Schmidt JH III: Tonsillar ectopia and Chiari malformations: monozygotic triplets. Case report. J Neurosurg 82:497–500, 1995
Coria F, , Quintana F, , Rebollo M, , Combarros O, & Berciano J: Occipital dysplasia and Chiari type I deformity in a family. J Neurol Sci 62:147–158, 1983
Fijisawa H, , Hasegawa M, , Kida S, & Yamashita J: A novel fibro-blast growth factor receptor 2 mutation in Crouzon syndrome associated with Chiari type I malformation and syringomyelia. J Neurosurg 97:396–400, 2002
Gripp KW, , Scott CI Jr, , Nicholson L, , Magram G, & Grissom LE: Chiari malformation and tonsillar ectopia in twin brothers and father with autosomal dominant spondylo-epiphyseal dysplasia tarda. Skeletal Radiol 26:131–133, 1997
Herman MD, , Cheek WR, & Storrs BB: Two siblings with the Chiari I malformation. Pediatr Neurosurg 16:183–184, 1991
Marin-Padilla M, & Marin-Padilla TM: Morphogenesis of experimentally induced Arnold–Chiari malformation. J Neurol Sci 50:29–55, 1981
Milhorat TH, , Chou MW, , Trinidad EM, , Kula RW, , Mandell M, & Wolpert C, et al.: Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients. Neurosurgery 44:1005–1017, 1999
Murphy RL, , Tubbs RS, , Grabb PA, & Oakes WJ: Chiari I malformation and idiopathic growth hormone deficiency in siblings. Childs Nerv Syst 22:632–634, 2006
Nishikawa M, , Sakamoto H, , Hakuba A, , Yasui T, , Kitano S, & Nakanishi N, et al.: Pathogenesis of Chiari malformation: a morphometric study of the posterior cranial fossa. J Neurosurg 86:40–47, 1997
Paquis P, , Lonjon M, , Brunet M, , Lambert JC, & Grellier P: Chiari Type I malformation and syringomyelia in unrelated patients with blepharophimosis. Report of two cases. J Neurosurg 89:835–838, 1998
Schimmenti LA, , Shim HH, , Wirtschafter JD, , Panzarino VA, , Kashtan CE, & Kirkpatrick SJ, et al.: Homonucleotide expansion and contraction mutations of PAX2 and inclusion of Chiari 1 malformation as part of renal-coloboma syndrome. Hum Mutat 14:369–376, 1999
Sgouros S, , Kountouri M, & Natarajan K: Posterior fossa volume in children with Chiari malformation Type I. J Neurosurg 105:2 Suppl 101–106, 2006
Speer MC, , Enterline DS, , Mehltretter L, , Hammock P, , Joseph J, & Dickerson M, et al.: Chiari type 1 malformation with or without syringomyelia: prevalence and genetics. J Gen Counsel 12:297–311, 2003
Speer MC, , George TM, , Enterline DS, , Franklin A, , Wolpert CM, & Milhorat TH: A genetic hypothesis for Chiari I malformation with or without syringomyelia. Neurosurg Focus 8:3 E12, 2000
Stovner JL, & Sjaastad O: Segmental hyperhidrosis in two siblings with Chiari type I malformation. Eur Neurol 35:149–155, 1995
Tubbs RS, , Bui CJ, , Rice WC, , Loukas M, , Naftel RP, & Holcombe MP, et al.: Critical analysis of the Chiari malformation Type I found in children with lipomyelomeningocele. J Neurosurg 106:3 Suppl 196–200, 2007
Tubbs RS, , Elton S, , Grabb P, , Dockery SE, , Bartolucci AA, & Oakes WJ: Analysis of the posterior fossa in children with the Chiari 0 malformation. Neurosurgery 48:1050–1054, 2001
Tubbs RS, , McGirt MJ, & Oakes WJ: Surgical experience in 130 pediatric patients with Chiari I malformations. J Neurosurg 99:291–296, 2003
Tubbs RS, , Webb D, , Abdullatif H, , Conklin M, , Doyle S, & Oakes WJ: Posterior cranial fossa volume in patients with rickets: insights into the increased occurrence of Chiari I malformation in metabolic bone disease. Neurosurgery 55:380–384, 2004
Tubbs RS, , Wellons JC III, , Blount JP, & Oakes WJ: Syringomyelia in twin brothers discordant for Chiari I malformation: case report. J Child Neurol 19:459–462, 2004
Tubbs RS, , Wellons JC III, , Smyth MD, , Bartolucci AA, , Blount JP, & Oakes WJ, et al.: Children with growth hormone deficiency and Chiari I malformation: a morphometric analysis of the posterior cranial fossa. Pediatr Neurosurg 38:324–328, 2003
Yabe I, , Kikuchi S, & Tashiro K: Familial syringomyelia: the first Japanese case and review of the literature. Clin Neurol Neurosurg 105:69–71, 2002
Zakeri A, , Glasauer FE, & Egnatchik JG: Familial syringomyelia: case report and review of the literature. Surg Neurol 44:48–53, 1995
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